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Noble-metal nanoframes consisting of interconnected, ultrathin ridges have received considerable attention in the field of heterogeneous catalysis. The enthusiasm arises from the high utilization efficiency of atoms for significantly reducing the material loading while enhancing the catalytic performance. In this review article, we offer a comprehensive assessment of research endeavors in the design and rational synthesis of noble-metal nanoframes for applications in catalysis. We start with a brief introduction to the unique characteristics of nanoframes, followed by a discussion of the synthetic strategies and their controls in terms of structure and composition. We then present case studies to elucidate mechanistic details behind the synthesis of mono-, bi-, and multimetallic nanoframes, as well as heterostructured and hybrid systems. We discuss their performance in electrocatalysis, thermal catalysis, and photocatalysis. Finally, we highlight recent progress in addressing the structural and compositional stability issues of nanoframes for the assurance of robustness in catalytic applications.

Silver is an excellent catalyst for oxidation reactions such as ethylene epoxidation, but it shows limited activity toward reduction reactions. Here we report a strategy to revitalize Ag nanocrystals as a redox catalyst for the production of an aromatic azo compound by modifying their surface with an isocyanide-based compound. We also leverage in situ fingerprint spectroscopy to acquire molecular insights into the reaction mechanism by probing the vibrational modes of all chemical species at the catalytic surface with surface-enhanced Raman spectroscopy. We establish that binding of isocyanide to Ag nanocrystals makes it possible for Ag to extract the oxygen atoms from the nitro-groups of nitroaromatics and then use these atoms to oxidize isocyanide to isocyanate. Concurrently, the coupling between two adjacent deoxygenated nitroaromatic molecules leads to the formation of an aromatic azo compound., Ag nanocrystals can serve as a redox catalyst for the production of an aromatic azo compound when their surface is modified with an isocyanide-based molecule.

We report an investigation of the adsorption of thiol and isocyanide molecules on colloidal Ag nanocubes through surface-enhanced Raman scattering (SERS). Specifically, we collect SERS spectra in situ at different time points from a mixture of Ag nanocubes and ligand molecules at a specific concentration. We demonstrate that 4-nitrothiophenol could readily bind to the Ag surface through strong thiol–Ag interaction. We also observe red shifts for the SERS peaks as the concentration decreases, suggesting a change to the molecular orientation relative to the surface. Likewise, 4-aminothiophenol also adsorbs onto Ag quickly, but gives much weaker SERS signals relative to 4-nitrothiophenol because the electron-donating amine group would retard the chemical enhancement of SERS. Different from thiols, 1,4-phenylene diisocyanide binds to Ag surface through a relatively weak, σ-donation bond. With an increase in concentration, molecules tend to adsorb on the nanocubes with the benzene ring tilting away from the su...

We report the defect-assisted deposition of Au on Ag nanocubes for the generation of Ag@Au core–shell nanocubes with three to eight atomic layers. In a standard protocol, we disperse Ag nanocubes in an ethylene glycol (EG) solution containing poly(vinylpyrrolidone) and then titrate aqueous HAuCl4 at 110 °C. Initially, the galvanic replacement reaction between HAuCl4 and Ag allows the deposition of Au on the edges of the nanocubes with highest surface energy as the Ag atoms on the side faces are dissolved into the aqueous suspension in the form of Ag(I) ions to create surface defects. These defects then become preferential sites for the codeposition of Ag and Au atoms derived from the coreduction of both the Ag(I) and Au(III) ions in the reaction solution by EG. Once the defect sites have been filled, the additional Ag and Au atoms will rapidly diffuse across the entire surface of each nanocube for the generation of a nanocube with a relatively thin shell made of a Ag–Au alloy. Afterward, the chemical redu...

We report the fabrication of Ag-Pd concave nanocrystals by introducing the Pd(ii) precursor into an aqueous suspension of Ag nanocubes in the presence of cetyltrimethylammonium chloride (CTAC) under ambient conditions. Different from the previously reported work that involved the oxidation of Ag and deposition of Pd at random sites on the surface for the generation of Ag-Pd hollow nanocrystals, we demonstrate that the Cl- ions from CTAC can confine the oxidation of Ag atoms to the side faces of a nanocube while the resultant Pd atoms are deposited on the edges in an orthogonal manner. By controlling the amount of the Pd(ii) precursor involved in a synthesis, we can transform Ag nanocubes into Ag-Pd nanocrystals with different degrees of concaveness for the side faces and controllable Pd contents. We characterize the outermost layer of concave surfaces for the as-obtained Ag-Pd nanocrystals by surface-enhanced Raman scattering (SERS) through the use of an isocyanide probe. This facile approach would enable the fabrication of Ag-based concave nanocrystals for applications in plasmonics and catalysis.

We report a simple and general method for the production of Ag–Rh bimetallic nanostructures with a unique integration of the plasmonic and catalytic properties exemplified by these two metals, respectively. When a Rh(III) precursor is titrated into a polyol suspension of Ag nanocubes held at 110 °C in the presence of ascorbic acid and poly(vinylpyrrolidone), Rh atoms are generated and deposited on the nanocubes. When the amount of Rh(III) precursor is relatively low, the Rh atoms tend to nucleate from the edges of the Ag nanocubes and then follow an island growth mode because of the relatively low temperature involved and the high cohesive energy of Rh. The Rh islands can be maintained with an ultrafine size of only several nanometers, presenting an extremely large specific surface area for catalytic applications. As the amount of Rh(III) precursor is increased, the galvanic replacement reaction between the Rh(III) and Ag nanocubes will kick in, leading to the formation of increasingly concaved side faces...

We report a facile synthesis of Ag nanocubes with concave side faces and Au–Ag alloy frames, namely Ag@Au–Ag concave nanocrystals, by titrating HAuCl4 solution into an aqueous mixture of Ag nanocubes, ascorbic acid (H2Asc), NaOH, and cetyltrimethylammonium chloride (CTAC) at an initial pH of 11.6 under ambient conditions. Different from all previous studies involving poly(vinylpyrrolidine), the use of CTAC at a sufficiently high concentration plays an essential role in carving away Ag atoms from the side faces through galvanic replacement. Concurrent co-deposition of Au and Ag atoms via chemical reduction at orthogonal sites on the surface of Ag nanocubes leads to the generation of Ag@Au–Ag concave nanocrystals with well-defined and controllable structures. Specifically, in the presence of CTAC-derived Cl– ions, the titrated HAuCl4 is maintained in the AuCl4– species, enabling its galvanic replacement with the Ag atoms located on the side faces of nanocubes. The released Ag+ ions can be retained in the so...

A facile method is described herein for generating a mineral gradient in a biodegradable polymer scaffold. The gradient is achieved by swelling a composite film made of polycaprolactone (PCL) and hydroxyapatite (HAp) nanoparticles with a PCL solution. During the swelling process, the solvent and PCL polymer chains diffuse into the composite film, generating a gradient in HAp density at their interface. The thickness of the mineral gradient can be tuned by varying the extent of swelling to match the length scale of the natural tendon-to-bone attachment (20-60 µm). When patterned with an array of funnel-shaped channels, the mineral gradient presents stem cells with spatial gradations in both biochemical cues (e.g., osteoinductivity and conductivity associated with the HAp nanoparticles) and mechanical cues (e.g., substrate stiffness) to stimulate their differentiation into a graded distribution of cell phenotypes. This new class of biomimetic scaffolds holds great promise for facilitating the regeneration of the injured tendon-to-bone attachment by stimulating the formation of a functionally graded interface.

We report a facile route to the synthesis of Ag@Au–Pt trimetallic nanocubes in which the Ag, Au, and Pt atoms are exposed at the corners, side faces, and edges, respectively. Our success relies on the use of Ag@Au nanocubes, with Ag2O patches at the corners and Au on the side faces and edges, as seeds for the site-selective deposition of Pt on the edges only in a reaction system containing ascorbic acid (H2Asc) and poly(vinylpyrrolidone). At an initial pH of 3.2, H2Asc can dissolve the Ag2O patches, exposing the Ag atoms at the corners of a nanocube. Upon the injection of the H2PtCl6 precursor, the Pt atoms derived from the reduction by both H2Asc and Ag are preferentially deposited on the edges, leading to the formation of Ag@Au–Pt trimetallic nanocubes. We demonstrate the use of 2,6-dimethylphenyl isocyanide as a molecular probe to confirm and monitor the deposition of Pt atoms on the edges of nanocubes through surface-enhanced Raman scattering (SERS). We further explore the use of these bifunctional trimetallic nanoparticles with integrated plasmonic and catalytic properties for in situ SERS monitoring the reduction of 4-nitrothiophenol by NaBH4. Upon the removal of Ag via H2O2 etching, the Ag@Au–Pt nanocubes evolve into trimetallic nanoboxes with a wall thickness of about 2 nm and well-defined openings at the corners. The trimetallic nanoboxes embrace plasmon resonance peaks in the near-infrared region with potential in biomedical applications.

We report the development of an isocyanide-based molecular probe for in situ characterizing the overgrowth of a second metal on silver nanocrystal seeds in solution by surface-enhanced Raman scattering (SERS). As the first demonstration, we elucidate that the vibrational frequency of 2,6-dimethylphenyl isocyanide (2,6-DMPI) can serve as a distinctive reporter for capturing the nucleation of Pt on the edges of Ag nanocubes in the aqueous solution containing a Pt precursor, ascorbic acid, and poly(vinylpyrrolidone) under ambient conditions. Our success relies on the difference in stretching frequency for the NC bond when the isocyanide group binds to the Ag and Pt atoms. Specifically, σ donation from the antibonding σ* orbital of the -NC group to the d-band of Ag would strengthen the NC bond, blue shifting the stretching frequency. In contrast, π-back-donation from the d-band of Pt to the π* antibonding orbital of the -NC group would weaken the NC bond, leading to a red shift of stretching frequency. Therefore, it is feasible to in situ characterize the outermost surface that consists of both newly deposited Pt atoms and remaining Ag atoms by following the stretching frequencies and intensities of 2,6-DMPI in real time. Because the SERS hot spots on the edges of Ag nanocubes coincide with the {110} facets preferred for the nucleation of Pt atoms, this technique is capable of resolving 27 Pt atoms being deposited on each edge of a 39 nm Ag nanocube in the original growth solution. Collectively, in situ SERS, with its consummate sensitivity to molecular structure and bonding of isocyanide-based molecular probe, could elucidate the mechanistic details involved in the seeded overgrowth of a catalytically significant metal, such as Pt, Pd, Ir, Rh, and Ru, on the surface of a Ag or Au nanocrystal seed.